Overexpression of CDC20 Confer a Poorer Prognosis in Bladder Cancer Identified by Gene Co-Expression Network Analysis

<b>Background/Objectives</b>: Bladder cancer (BCa) ranks as the tenth most prevalent malignancy worldwide, characterized by high morbidity and mortality rates. Despite advancements in understanding its pathogenesis, the identification of robust prognostic biomarkers remains critical for improving clinical outcomes. This study aims to identify and validate novel prognostic markers for BCa through integrated bioinformatics and experimental approaches. <b>Methods</b>: Gene expression data and clinical information were obtained from the GEO (GSE13507) and TCGA databases. Differential gene expression analysis and weighted gene co-expression network analysis (WGCNA) were employed to identify overlapping genes. Functional enrichment analysis was performed to explore biological functions, followed by protein-protein interaction (PPI) network construction and survival analysis. Key candidate genes were screened using the CytoHubba plugin in Cytoscape. <i>CDC20</i> expression was validated through RT-qPCR, and its functional role in BCa cells was assessed in vitro. <b>Results</b>: Eight candidate hub genes (<i>TROAP</i>, <i>TPX2</i>, <i>TOP2A</i>, <i>KIF2C</i>, <i>AURKA</i>, <i>CDC20</i>, <i>PRC1</i>, and <i>AURKB</i>) were identified. Survival analysis revealed that high <i>CDC20</i> expression was significantly associated with decreased overall survival in BCa patients. Mechanistic investigations demonstrated that <i>CDC20</i> promotes tumor invasion and growth by modulating mitosis and cell cycle progression, while also influencing the tumor microenvironment through immune cell regulation. Experimental validation confirmed the tumor-promoting role of <i>CDC20</i> in BCa cells. <b>Conclusions</b>: This study identifies <i>CDC20</i> as a key prognostic biomarker for bladder cancer, providing novel insights for early diagnosis, clinical treatment, and prognosis assessment. The findings highlight the potential of <i>CDC20</i> as a therapeutic target and underscore the value of integrated bioinformatics and experimental validation in biomarker discovery.

Authors

Institutions

Publication Details

Journal
Diagnostics
Published
2025-11-27
DOI
https://doi.org/10.3390/diagnostics15233016
Primary Topic
Ferroptosis and cancer prognosis
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Overexpression of CDC20 Confer a Poorer Prognosis in Bladder Cancer Identified by Gene Co-Expression Network Analysis

Lanyu Wang, Xiangliang Yang, Wei Tian, Xiaojie Lu et al.
Diagnostics
Ferroptosis and cancer prognosis
article

Overexpression of CDC20 Confer a Poorer Prognosis in Bladder Cancer Identified by Gene Co-Expression Network Analysis

Lanyu Wang, Xiangliang Yang, Wei Tian, Xiaojie Lu, Zengli Miao, Jun Ruan, Yunhai Guo
article en

Abstract

<b>Background/Objectives</b>: Bladder cancer (BCa) ranks as the tenth most prevalent malignancy worldwide, characterized by high morbidity and mortality rates. Despite advancements in understanding its pathogenesis, the identification of robust prognostic biomarkers remains critical for improving clinical outcomes. This study aims to identify and validate novel prognostic markers for BCa through integrated bioinformatics and experimental approaches. <b>Methods</b>: Gene expression data and clinical information were obtained from the GEO (GSE13507) and TCGA databases. Differential gene expression analysis and weighted gene co-expression network analysis (WGCNA) were employed to identify overlapping genes. Functional enrichment analysis was performed to explore biological functions, followed by protein-protein interaction (PPI) network construction and survival analysis. Key candidate genes were screened using the CytoHubba plugin in Cytoscape. <i>CDC20</i> expression was validated through RT-qPCR, and its functional role in BCa cells was assessed in vitro. <b>Results</b>: Eight candidate hub genes (<i>TROAP</i>, <i>TPX2</i>, <i>TOP2A</i>, <i>KIF2C</i>, <i>AURKA</i>, <i>CDC20</i>, <i>PRC1</i>, and <i>AURKB</i>) were identified. Survival analysis revealed that high <i>CDC20</i> expression was significantly associated with decreased overall survival in BCa patients. Mechanistic investigations demonstrated that <i>CDC20</i> promotes tumor invasion and growth by modulating mitosis and cell cycle progression, while also influencing the tumor microenvironment through immune cell regulation. Experimental validation confirmed the tumor-promoting role of <i>CDC20</i> in BCa cells. <b>Conclusions</b>: This study identifies <i>CDC20</i> as a key prognostic biomarker for bladder cancer, providing novel insights for early diagnosis, clinical treatment, and prognosis assessment. The findings highlight the potential of <i>CDC20</i> as a therapeutic target and underscore the value of integrated bioinformatics and experimental validation in biomarker discovery.

DiagnosticsVol. 15(23)
Jiangnan University (CN), Nanchang University (CN), Tianjin Medical University General Hospital (CN), Wuxi No.2 People's Hospital (CN), Wuxi People's Hospital (CN), First Affiliated Hospital of Nanchang University (CN), Wuxi Institute of Technology (CN)
Openalex Percentile: Top 45%
Ferroptosis and cancer prognosis
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.